Encapsulation of isoquinoline in a polymer nanocontainer based on the CU-2-4 sulfocationite

H. Altshuler, G. Shkurenko, S. Lyrschikov
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引用次数: 1

Abstract

The possibility of the encapsulation of isoquinoline in the nanocontainer on the matrix of the sulfonated copolymer based on styrene and divinylbenzene (CU-2-4 sulfocationite) has been researched. The encapsulation of isoquinoline in the nanocontainer on polymer matrix was performed by ion-exchange sorption from aqueous solutions. CU-2-4 sulfocationite in hydrogen and isoquinoline forms was studied by NMR and Fourier IR spectroscopy. In the 13C NMR spectra of solid-state samples of the CU-2-4 cation exchanger in the isoquinoline form is observed additional resonance absorption band of 13C in the range of chemical shift 136 ppm, corresponding to the nodal carbon atom of the pyridine ring. The IR spectrum of the polymer containing the encapsulated isoquinoline be observed bands characteristic for skeletal vibrations in the area of isoquinoline fingerprints (1300-1600 cm-1) and the band of 938 cm-1 that corresponds to the deformation vibrations of the CH-group of pyridine ring, which is not in the spectrum of the H-form sulfocationite. The ion-exchange capacity of the nanocontainer based on СU-2-4 sulfocationite for isoquinoline was 5.5 meq/g. This corresponds to the content of ionogenic groups in the polymer. The dynamic ion-exchange capacity of sulfonated CU-2-4 cation exchanger during encapsulation of isoquinoline coincides with the ion-exchange capacity of sulfonated cation exchanger upon the release of isoquinoline from the polymer nanocontainer. The content of immobilized isoquinoline in the nanocontainer on the СU-2-4 matrix reaches 71 % by weight of the polymer. It is shown that isoquinoline is encapsulated and desorbed with the solution of hydrochloric acid at the same rate. Encapsulated isoquinoline is completely released from the polymer by desorption with the aqueous hydrochloric acid solution. The half-life during sorption and desorption (release) of isoquinoline is approximately 400 seconds. It is shown that the encapsulated isoquinoline to be completely released from the polymer by desorption with an aqueous hydrochloric acid solution. The kinetics of the encapsulation and release of isoquinoline from the nanocontainer based on CU-2-4 sulfocationite is determined by its diffusion in the polymer phase.
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CU-2-4硫酸盐基聚合物纳米容器中异喹啉的包封
研究了异喹啉在苯乙烯-二乙烯基苯磺化共聚物(CU-2-4磺化矿)为基体的纳米容器中包封的可能性。采用离子交换吸附法将异喹啉包封在聚合物基纳米容器中。用核磁共振和傅立叶红外光谱研究了氢和异喹啉形式的CU-2-4硫酸盐。在异喹啉形式CU-2-4阳离子交换剂固态样品的13C NMR光谱中,在136ppm的化学位移范围内观察到13C的附加共振吸收带,对应于吡啶环的节点碳原子。包覆异喹啉聚合物的红外光谱在异喹啉指纹区(1300 ~ 1600 cm-1)观察到骨架振动的特征波段,在h型磺化矿的光谱中观察到938 cm-1对应于吡啶环ch -基的变形振动波段。基于СU-2-4磺化矿的异喹啉纳米容器的离子交换容量为5.5 meq/g。这对应于聚合物中离子生成基团的含量。磺化CU-2-4阳离子交换剂在异喹啉包封过程中的动态离子交换容量与磺化阳离子交换剂在异喹啉从聚合物纳米容器中释放时的动态离子交换容量一致。在СU-2-4基质上的纳米容器中,固定化异喹啉的含量达到聚合物重量的71%。结果表明,异喹啉在盐酸溶液中以相同的速率被包封和解吸。包封的异喹啉通过盐酸水溶液解吸从聚合物中完全释放出来。异喹啉的吸附和解吸(释放)半衰期约为400秒。结果表明,包封后的异喹啉可以通过盐酸水溶液解吸从聚合物中完全释放出来。异喹啉在CU-2-4硫酸盐基纳米容器中的包封和释放动力学是由其在聚合物相中的扩散决定的。
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